Protein ID | Hirsu2|3651 |
Gene name | |
Location | Contig_1978:1696..3634 |
Strand | + |
Gene length (bp) | 1938 |
Transcript length (bp) | 1647 |
Coding sequence length (bp) | 1647 |
Protein length (aa) | 549 |
PFAM Domain ID | Short name | Long name | E-value | Start | End |
---|---|---|---|---|---|
PF02776 | TPP_enzyme_N | Thiamine pyrophosphate enzyme, N-terminal TPP binding domain | 8.9E-29 | 2 | 160 |
PF00205 | TPP_enzyme_M | Thiamine pyrophosphate enzyme, central domain | 1.8E-21 | 185 | 297 |
PF02775 | TPP_enzyme_C | Thiamine pyrophosphate enzyme, C-terminal TPP binding domain | 1.2E-11 | 383 | 461 |
Swissprot ID | Swissprot Description | Start | End | E-value |
---|---|---|---|---|
sp|Q4WXX9|PDC_ASPFU | Pyruvate decarboxylase OS=Neosartorya fumigata (strain ATCC MYA-4609 / Af293 / CBS 101355 / FGSC A1100) GN=pdcA PE=3 SV=1 | 1 | 544 | 0.0E+00 |
sp|P87208|PDC_EMENI | Pyruvate decarboxylase OS=Emericella nidulans (strain FGSC A4 / ATCC 38163 / CBS 112.46 / NRRL 194 / M139) GN=pdcA PE=3 SV=3 | 1 | 544 | 0.0E+00 |
sp|Q0CNV1|PDC_ASPTN | Pyruvate decarboxylase OS=Aspergillus terreus (strain NIH 2624 / FGSC A1156) GN=pdcA PE=3 SV=1 | 1 | 545 | 0.0E+00 |
sp|Q2UKV4|PDC_ASPOR | Pyruvate decarboxylase OS=Aspergillus oryzae (strain ATCC 42149 / RIB 40) GN=pdcA PE=3 SV=1 | 1 | 544 | 0.0E+00 |
sp|Q09737|PDC1_SCHPO | Putative pyruvate decarboxylase C13A11.06 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=SPAC13A11.06 PE=3 SV=2 | 1 | 546 | 0.0E+00 |
Swissprot ID | Swissprot Description | Start | End | E-value |
---|---|---|---|---|
sp|Q4WXX9|PDC_ASPFU | Pyruvate decarboxylase OS=Neosartorya fumigata (strain ATCC MYA-4609 / Af293 / CBS 101355 / FGSC A1100) GN=pdcA PE=3 SV=1 | 1 | 544 | 0.0E+00 |
sp|P87208|PDC_EMENI | Pyruvate decarboxylase OS=Emericella nidulans (strain FGSC A4 / ATCC 38163 / CBS 112.46 / NRRL 194 / M139) GN=pdcA PE=3 SV=3 | 1 | 544 | 0.0E+00 |
sp|Q0CNV1|PDC_ASPTN | Pyruvate decarboxylase OS=Aspergillus terreus (strain NIH 2624 / FGSC A1156) GN=pdcA PE=3 SV=1 | 1 | 545 | 0.0E+00 |
sp|Q2UKV4|PDC_ASPOR | Pyruvate decarboxylase OS=Aspergillus oryzae (strain ATCC 42149 / RIB 40) GN=pdcA PE=3 SV=1 | 1 | 544 | 0.0E+00 |
sp|Q09737|PDC1_SCHPO | Putative pyruvate decarboxylase C13A11.06 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=SPAC13A11.06 PE=3 SV=2 | 1 | 546 | 0.0E+00 |
sp|Q6FJA3|PDC1_CANGA | Pyruvate decarboxylase OS=Candida glabrata (strain ATCC 2001 / CBS 138 / JCM 3761 / NBRC 0622 / NRRL Y-65) GN=PDC1 PE=3 SV=1 | 3 | 548 | 8.0E-173 |
sp|P34734|PDC_HANUV | Pyruvate decarboxylase OS=Hanseniaspora uvarum GN=PDC PE=3 SV=1 | 1 | 548 | 1.0E-172 |
sp|O42873|PDC4_SCHPO | Putative pyruvate decarboxylase C3G9.11c OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=SPAC3G9.11c PE=3 SV=1 | 1 | 546 | 2.0E-170 |
sp|P16467|PDC5_YEAST | Pyruvate decarboxylase isozyme 2 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=PDC5 PE=1 SV=4 | 5 | 546 | 4.0E-170 |
sp|P33149|PDC1_KLUMA | Pyruvate decarboxylase OS=Kluyveromyces marxianus GN=PDC1 PE=3 SV=1 | 3 | 548 | 4.0E-169 |
sp|P26263|PDC6_YEAST | Pyruvate decarboxylase isozyme 3 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=PDC6 PE=1 SV=3 | 1 | 546 | 1.0E-168 |
sp|P06169|PDC1_YEAST | Pyruvate decarboxylase isozyme 1 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=PDC1 PE=1 SV=7 | 3 | 546 | 1.0E-167 |
sp|Q12629|PDC1_KLULA | Pyruvate decarboxylase OS=Kluyveromyces lactis (strain ATCC 8585 / CBS 2359 / DSM 70799 / NBRC 1267 / NRRL Y-1140 / WM37) GN=PDC1 PE=1 SV=2 | 3 | 546 | 1.0E-166 |
sp|P83779|PDC1_CANAL | Pyruvate decarboxylase OS=Candida albicans (strain SC5314 / ATCC MYA-2876) GN=PDC11 PE=1 SV=2 | 1 | 546 | 8.0E-158 |
sp|Q07471|THI3_YEAST | Thiamine metabolism regulatory protein THI3 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=THI3 PE=1 SV=1 | 1 | 534 | 1.0E-140 |
sp|P51844|PDC_ASPPA | Pyruvate decarboxylase OS=Aspergillus parasiticus GN=pdcA PE=3 SV=1 | 1 | 534 | 1.0E-110 |
sp|Q9CBD6|KDC_MYCLE | Alpha-keto-acid decarboxylase OS=Mycobacterium leprae (strain TN) GN=kdc PE=3 SV=1 | 1 | 544 | 8.0E-105 |
sp|Q742Q2|KDC_MYCPA | Alpha-keto-acid decarboxylase OS=Mycobacterium paratuberculosis (strain ATCC BAA-968 / K-10) GN=kdc PE=3 SV=1 | 1 | 534 | 2.0E-101 |
sp|A0QBE6|KDC_MYCA1 | Alpha-keto-acid decarboxylase OS=Mycobacterium avium (strain 104) GN=kdc PE=3 SV=2 | 1 | 534 | 1.0E-100 |
sp|P23234|DCIP_ENTCL | Indole-3-pyruvate decarboxylase OS=Enterobacter cloacae GN=ipdC PE=1 SV=1 | 2 | 545 | 3.0E-97 |
sp|P9WG37|KDC_MYCTU | Alpha-keto-acid decarboxylase OS=Mycobacterium tuberculosis (strain ATCC 25618 / H37Rv) GN=kdc PE=1 SV=1 | 1 | 533 | 2.0E-96 |
sp|A5U0P1|KDC_MYCTA | Alpha-keto-acid decarboxylase OS=Mycobacterium tuberculosis (strain ATCC 25177 / H37Ra) GN=kdc PE=3 SV=1 | 1 | 533 | 2.0E-96 |
sp|A1KGY5|KDC_MYCBP | Alpha-keto-acid decarboxylase OS=Mycobacterium bovis (strain BCG / Pasteur 1173P2) GN=kdc PE=3 SV=1 | 1 | 533 | 2.0E-96 |
sp|Q7U140|KDC_MYCBO | Alpha-keto-acid decarboxylase OS=Mycobacterium bovis (strain ATCC BAA-935 / AF2122/97) GN=kdc PE=3 SV=1 | 1 | 533 | 2.0E-96 |
sp|P9WG36|KDC_MYCTO | Alpha-keto-acid decarboxylase OS=Mycobacterium tuberculosis (strain CDC 1551 / Oshkosh) GN=kdc PE=3 SV=1 | 1 | 533 | 1.0E-95 |
sp|A0R480|KDC_MYCS2 | Alpha-keto-acid decarboxylase OS=Mycobacterium smegmatis (strain ATCC 700084 / mc(2)155) GN=kdc PE=3 SV=1 | 1 | 546 | 6.0E-93 |
sp|A0PL16|KDC_MYCUA | Alpha-keto-acid decarboxylase OS=Mycobacterium ulcerans (strain Agy99) GN=kdc PE=3 SV=1 | 1 | 533 | 1.0E-90 |
sp|Q06408|ARO10_YEAST | Transaminated amino acid decarboxylase OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=ARO10 PE=1 SV=1 | 4 | 546 | 4.0E-81 |
sp|Q92345|PDC2_SCHPO | Probable pyruvate decarboxylase C1F8.07c OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=SPAC1F8.07c PE=1 SV=3 | 1 | 546 | 2.0E-80 |
sp|A2Y5L9|PDC1_ORYSI | Pyruvate decarboxylase 1 OS=Oryza sativa subsp. indica GN=PDC1 PE=2 SV=1 | 1 | 546 | 8.0E-80 |
sp|Q9M040|PDC4_ARATH | Pyruvate decarboxylase 4 OS=Arabidopsis thaliana GN=PDC4 PE=2 SV=1 | 2 | 546 | 2.0E-79 |
sp|Q0DHF6|PDC1_ORYSJ | Pyruvate decarboxylase 1 OS=Oryza sativa subsp. japonica GN=PDC1 PE=2 SV=1 | 1 | 546 | 3.0E-79 |
sp|P28516|PDC1_MAIZE | Pyruvate decarboxylase 1 OS=Zea mays GN=PDC1 PE=2 SV=1 | 1 | 546 | 1.0E-78 |
sp|Q9M039|PDC3_ARATH | Pyruvate decarboxylase 3 OS=Arabidopsis thaliana GN=PDC3 PE=2 SV=1 | 2 | 546 | 2.0E-77 |
sp|Q9P7P6|PDC3_SCHPO | Probable pyruvate decarboxylase C186.09 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=SPAC186.09 PE=3 SV=1 | 2 | 534 | 2.0E-76 |
sp|P51846|PDC2_TOBAC | Pyruvate decarboxylase 2 OS=Nicotiana tabacum GN=PDC2 PE=2 SV=1 | 1 | 546 | 2.0E-75 |
sp|O82647|PDC1_ARATH | Pyruvate decarboxylase 1 OS=Arabidopsis thaliana GN=PDC1 PE=2 SV=1 | 2 | 546 | 6.0E-75 |
sp|A2XFI3|PDC2_ORYSI | Pyruvate decarboxylase 2 OS=Oryza sativa subsp. indica GN=PDC2 PE=2 SV=2 | 1 | 546 | 3.0E-74 |
sp|Q9FFT4|PDC2_ARATH | Pyruvate decarboxylase 2 OS=Arabidopsis thaliana GN=PDC2 PE=2 SV=1 | 1 | 546 | 2.0E-73 |
sp|Q10MW3|PDC2_ORYSJ | Pyruvate decarboxylase 2 OS=Oryza sativa subsp. japonica GN=PDC2 PE=2 SV=1 | 1 | 546 | 4.0E-73 |
sp|P51850|PDC1_PEA | Pyruvate decarboxylase 1 OS=Pisum sativum GN=PDC1 PE=2 SV=1 | 1 | 546 | 4.0E-70 |
sp|A2YQ76|PDC3_ORYSI | Pyruvate decarboxylase 3 OS=Oryza sativa subsp. indica GN=PDC3 PE=3 SV=2 | 1 | 546 | 4.0E-68 |
sp|Q0D3D2|PDC3_ORYSJ | Pyruvate decarboxylase 3 OS=Oryza sativa subsp. japonica GN=PDC3 PE=2 SV=1 | 1 | 546 | 4.0E-68 |
sp|P33287|PDC_NEUCR | Pyruvate decarboxylase OS=Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) GN=cfp PE=1 SV=1 | 1 | 546 | 4.0E-67 |
sp|P06672|PDC_ZYMMO | Pyruvate decarboxylase OS=Zymomonas mobilis subsp. mobilis (strain ATCC 31821 / ZM4 / CP4) GN=pdc PE=1 SV=1 | 1 | 487 | 1.0E-55 |
sp|P51845|PDC1_TOBAC | Pyruvate decarboxylase 1 (Fragment) OS=Nicotiana tabacum GN=PDC1 PE=2 SV=1 | 40 | 458 | 2.0E-44 |
sp|P51852|DCIP_AZOBR | Indole-3-pyruvate decarboxylase OS=Azospirillum brasilense GN=ipdC PE=1 SV=1 | 2 | 526 | 7.0E-39 |
sp|P51851|PDC2_PEA | Pyruvate decarboxylase 2 (Fragment) OS=Pisum sativum GN=PDC2 PE=2 SV=1 | 191 | 546 | 6.0E-34 |
sp|Q05327|PDC3_MAIZE | Pyruvate decarboxylase 3 (Fragment) OS=Zea mays GN=PDC3 PE=2 SV=1 | 360 | 546 | 7.0E-27 |
sp|Q9LF46|HACL_ARATH | 2-hydroxyacyl-CoA lyase OS=Arabidopsis thaliana GN=HACL PE=1 SV=1 | 25 | 509 | 4.0E-21 |
sp|O78518|ILVB_GUITH | Acetolactate synthase large subunit OS=Guillardia theta GN=ilvB PE=3 SV=1 | 2 | 509 | 4.0E-20 |
sp|Q9QXE0|HACL1_MOUSE | 2-hydroxyacyl-CoA lyase 1 OS=Mus musculus GN=Hacl1 PE=1 SV=2 | 23 | 509 | 5.0E-20 |
sp|Q8CHM7|HACL1_RAT | 2-hydroxyacyl-CoA lyase 1 OS=Rattus norvegicus GN=Hacl1 PE=1 SV=1 | 23 | 509 | 1.0E-18 |
sp|Q57725|ILVB_METJA | Probable acetolactate synthase large subunit OS=Methanocaldococcus jannaschii (strain ATCC 43067 / DSM 2661 / JAL-1 / JCM 10045 / NBRC 100440) GN=ilvB PE=3 SV=1 | 2 | 455 | 8.0E-18 |
sp|D5AKX8|XSC_RHOCB | Sulfoacetaldehyde acetyltransferase OS=Rhodobacter capsulatus (strain ATCC BAA-309 / NBRC 16581 / SB1003) GN=xsc PE=2 SV=1 | 2 | 515 | 6.0E-17 |
sp|P37251|ILVB_BACSU | Acetolactate synthase large subunit OS=Bacillus subtilis (strain 168) GN=ilvB PE=1 SV=4 | 3 | 454 | 9.0E-17 |
sp|Q9UJ83|HACL1_HUMAN | 2-hydroxyacyl-CoA lyase 1 OS=Homo sapiens GN=HACL1 PE=1 SV=2 | 23 | 503 | 5.0E-16 |
sp|Q9RQ65|ILVI_BUCSC | Acetolactate synthase large subunit OS=Buchnera aphidicola subsp. Schlechtendalia chinensis GN=ilvI PE=3 SV=1 | 2 | 457 | 1.0E-15 |
sp|P27868|ILVB_ARTPT | Acetolactate synthase (Fragment) OS=Arthrospira platensis GN=ilvY PE=3 SV=1 | 2 | 457 | 1.0E-14 |
sp|P0A623|ILVB_MYCBO | Acetolactate synthase OS=Mycobacterium bovis (strain ATCC BAA-935 / AF2122/97) GN=ilvB PE=3 SV=1 | 1 | 456 | 1.0E-14 |
sp|P9WG41|ILVB1_MYCTU | Acetolactate synthase large subunit IlvB1 OS=Mycobacterium tuberculosis (strain ATCC 25618 / H37Rv) GN=ilvB1 PE=1 SV=1 | 1 | 456 | 1.0E-14 |
sp|P9WG40|ILVB1_MYCTO | Acetolactate synthase large subunit IlvB1 OS=Mycobacterium tuberculosis (strain CDC 1551 / Oshkosh) GN=ilvB1 PE=3 SV=1 | 1 | 456 | 1.0E-14 |
sp|O33112|ILVB_MYCLE | Acetolactate synthase OS=Mycobacterium leprae (strain TN) GN=ilvB PE=3 SV=1 | 1 | 456 | 5.0E-14 |
sp|Q0JMH0|HACL_ORYSJ | 2-hydroxyacyl-CoA lyase OS=Oryza sativa subsp. japonica GN=Os01g0505400 PE=3 SV=3 | 53 | 509 | 1.0E-13 |
sp|Q92EQ4|IOLD_LISIN | 3D-(3,5/4)-trihydroxycyclohexane-1,2-dione hydrolase OS=Listeria innocua serovar 6a (strain CLIP 11262) GN=iolD PE=3 SV=1 | 26 | 517 | 2.0E-13 |
sp|O85293|ILVI_BUCAP | Acetolactate synthase large subunit OS=Buchnera aphidicola subsp. Schizaphis graminum (strain Sg) GN=ilvI PE=3 SV=1 | 2 | 454 | 2.0E-13 |
sp|Q84H41|XSC_ALCXX | Sulfoacetaldehyde acetyltransferase OS=Alcaligenes xylosoxydans xylosoxydans GN=xsc PE=1 SV=3 | 2 | 461 | 4.0E-13 |
sp|O08353|ILVB_METAO | Probable acetolactate synthase large subunit OS=Methanococcus aeolicus GN=ilvB PE=3 SV=1 | 3 | 491 | 4.0E-13 |
sp|P00893|ILVI_ECOLI | Acetolactate synthase isozyme 3 large subunit OS=Escherichia coli (strain K12) GN=ilvI PE=1 SV=2 | 2 | 457 | 4.0E-13 |
sp|P40811|ILVI_SALTY | Acetolactate synthase isozyme 3 large subunit OS=Salmonella typhimurium (strain LT2 / SGSC1412 / ATCC 700720) GN=ilvI PE=3 SV=3 | 2 | 455 | 1.0E-12 |
sp|P00892|ILVG_ECOLI | Acetolactate synthase isozyme 2 large subunit OS=Escherichia coli (strain K12) GN=ilvG PE=1 SV=3 | 2 | 461 | 2.0E-12 |
sp|O06335|ILVB2_MYCTU | Putative acetolactate synthase large subunit IlvB2 OS=Mycobacterium tuberculosis (strain ATCC 25618 / H37Rv) GN=ilvB2 PE=2 SV=1 | 2 | 456 | 3.0E-12 |
sp|Q89AP7|ILVI_BUCBP | Acetolactate synthase large subunit OS=Buchnera aphidicola subsp. Baizongia pistaciae (strain Bp) GN=ilvI PE=3 SV=1 | 2 | 457 | 3.0E-12 |
sp|Q84H44|XSC_CASDE | Sulfoacetaldehyde acetyltransferase OS=Castellaniella defragrans GN=xsc PE=1 SV=3 | 2 | 461 | 3.0E-12 |
sp|P45261|ILVI_HAEIN | Acetolactate synthase large subunit OS=Haemophilus influenzae (strain ATCC 51907 / DSM 11121 / KW20 / Rd) GN=ilvI PE=3 SV=1 | 2 | 457 | 4.0E-12 |
sp|Q59498|ILVB_MYCAV | Acetolactate synthase OS=Mycobacterium avium GN=ilvB PE=3 SV=1 | 1 | 456 | 6.0E-12 |
sp|Q9LCV9|CEAS_STRCL | N(2)-(2-carboxyethyl)arginine synthase OS=Streptomyces clavuligerus GN=ceaS PE=1 SV=1 | 25 | 487 | 6.0E-12 |
sp|P42463|ILVB_CORGL | Acetolactate synthase large subunit OS=Corynebacterium glutamicum (strain ATCC 13032 / DSM 20300 / JCM 1318 / LMG 3730 / NCIMB 10025) GN=ilvB PE=3 SV=1 | 6 | 456 | 3.0E-11 |
sp|P27696|ILVB_KLEPN | Acetolactate synthase, catabolic OS=Klebsiella pneumoniae GN=budB PE=1 SV=1 | 2 | 459 | 8.0E-11 |
sp|P96591|YDAP_BACSU | Putative thiamine pyrophosphate-containing protein YdaP OS=Bacillus subtilis (strain 168) GN=ydaP PE=2 SV=1 | 2 | 454 | 2.0E-10 |
sp|P08142|ILVB_ECOLI | Acetolactate synthase isozyme 1 large subunit OS=Escherichia coli (strain K12) GN=ilvB PE=1 SV=1 | 2 | 459 | 2.0E-10 |
sp|P57321|ILVI_BUCAI | Acetolactate synthase large subunit OS=Buchnera aphidicola subsp. Acyrthosiphon pisum (strain APS) GN=ilvI PE=3 SV=1 | 2 | 454 | 2.0E-10 |
sp|Q04789|ILVX_BACSU | Acetolactate synthase OS=Bacillus subtilis (strain 168) GN=alsS PE=2 SV=3 | 2 | 480 | 2.0E-10 |
sp|Q58077|Y663_METJA | Uncharacterized protein MJ0663 OS=Methanocaldococcus jannaschii (strain ATCC 43067 / DSM 2661 / JAL-1 / JCM 10045 / NBRC 100440) GN=MJ0663 PE=3 SV=1 | 3 | 474 | 2.0E-10 |
sp|Q723S8|IOLD_LISMF | 3D-(3,5/4)-trihydroxycyclohexane-1,2-dione hydrolase OS=Listeria monocytogenes serotype 4b (strain F2365) GN=iolD PE=3 SV=2 | 26 | 526 | 5.0E-10 |
sp|Q92UW6|XSC_RHIME | Probable sulfoacetaldehyde acetyltransferase OS=Rhizobium meliloti (strain 1021) GN=xsc PE=3 SV=1 | 2 | 452 | 7.0E-10 |
sp|P14874|ILVB2_BRANA | Acetolactate synthase 2, chloroplastic OS=Brassica napus PE=3 SV=1 | 33 | 454 | 1.0E-09 |
sp|Q02137|ILVB_LACLA | Acetolactate synthase large subunit OS=Lactococcus lactis subsp. lactis (strain IL1403) GN=ilvB PE=3 SV=2 | 1 | 461 | 2.0E-09 |
sp|P27818|ILVB1_BRANA | Acetolactate synthase 1, chloroplastic OS=Brassica napus PE=3 SV=1 | 2 | 454 | 2.0E-09 |
sp|P27819|ILVB3_BRANA | Acetolactate synthase 3, chloroplastic OS=Brassica napus PE=3 SV=1 | 2 | 454 | 2.0E-09 |
sp|P09342|ILVB1_TOBAC | Acetolactate synthase 1, chloroplastic OS=Nicotiana tabacum GN=ALS SURA PE=1 SV=1 | 2 | 454 | 4.0E-09 |
sp|P09114|ILVB2_TOBAC | Acetolactate synthase 2, chloroplastic OS=Nicotiana tabacum GN=ALS SURB PE=1 SV=1 | 2 | 454 | 4.0E-09 |
sp|Q5KYR0|IOLD_GEOKA | 3D-(3,5/4)-trihydroxycyclohexane-1,2-dione hydrolase OS=Geobacillus kaustophilus (strain HTA426) GN=iolD PE=3 SV=1 | 33 | 457 | 1.0E-08 |
sp|Q8Y9Y1|IOLD_LISMO | 3D-(3,5/4)-trihydroxycyclohexane-1,2-dione hydrolase OS=Listeria monocytogenes serovar 1/2a (strain ATCC BAA-679 / EGD-e) GN=iolD PE=3 SV=1 | 33 | 517 | 2.0E-08 |
sp|P17597|ILVB_ARATH | Acetolactate synthase, chloroplastic OS=Arabidopsis thaliana GN=ALS PE=1 SV=1 | 2 | 454 | 2.0E-08 |
sp|Q5WKY8|IOLD_BACSK | 3D-(3,5/4)-trihydroxycyclohexane-1,2-dione hydrolase OS=Bacillus clausii (strain KSM-K16) GN=iolD PE=3 SV=1 | 28 | 526 | 2.0E-08 |
sp|Q54DA9|HACL1_DICDI | Probable 2-hydroxyacyl-CoA lyase 1 OS=Dictyostelium discoideum GN=hacl1 PE=3 SV=1 | 25 | 470 | 2.0E-08 |
sp|Q7U5G1|ILVB_SYNPX | Acetolactate synthase large subunit OS=Synechococcus sp. (strain WH8102) GN=ilvB PE=3 SV=1 | 2 | 454 | 3.0E-08 |
sp|A4IPB6|IOLD_GEOTN | 3D-(3,5/4)-trihydroxycyclohexane-1,2-dione hydrolase OS=Geobacillus thermodenitrificans (strain NG80-2) GN=iolD PE=3 SV=1 | 33 | 457 | 5.0E-08 |
sp|P40149|OXC_OXAFO | Oxalyl-CoA decarboxylase OS=Oxalobacter formigenes GN=oxc PE=1 SV=1 | 25 | 240 | 7.0E-08 |
sp|P07342|ILVB_YEAST | Acetolactate synthase catalytic subunit, mitochondrial OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=ILV2 PE=1 SV=1 | 3 | 454 | 1.0E-07 |
sp|P0CH62|CHDH_AZOSP | Cyclohexane-1,2-dione hydrolase OS=Azoarcus sp. PE=1 SV=1 | 24 | 457 | 2.0E-07 |
sp|P0AFI0|OXC_ECOLI | Oxalyl-CoA decarboxylase OS=Escherichia coli (strain K12) GN=oxc PE=1 SV=1 | 54 | 240 | 6.0E-06 |
sp|P0AFI1|OXC_ECO57 | Oxalyl-CoA decarboxylase OS=Escherichia coli O157:H7 GN=oxc PE=3 SV=1 | 54 | 240 | 6.0E-06 |
sp|Q9HUI8|ARUI_PSEAE | Probable 2-ketoarginine decarboxylase AruI OS=Pseudomonas aeruginosa (strain ATCC 15692 / PAO1 / 1C / PRS 101 / LMG 12228) GN=aruI PE=1 SV=1 | 2 | 454 | 7.0E-06 |
GO Term | Description | Terminal node |
---|---|---|
GO:0000287 | magnesium ion binding | Yes |
GO:0003824 | catalytic activity | Yes |
GO:0030976 | thiamine pyrophosphate binding | Yes |
GO:0036094 | small molecule binding | No |
GO:0043168 | anion binding | No |
GO:0019842 | vitamin binding | No |
GO:0097159 | organic cyclic compound binding | No |
GO:0046872 | metal ion binding | No |
GO:1901363 | heterocyclic compound binding | No |
GO:0005488 | binding | No |
GO:0043167 | ion binding | No |
GO:1901681 | sulfur compound binding | No |
GO:0043169 | cation binding | No |
GO:0003674 | molecular_function | No |
GO:0050997 | quaternary ammonium group binding | No |
Localizations | Signals | Cytoplasm | Nucleus | Extracellular | Cell membrane | Mitochondrion | Plastid | Endoplasmic reticulum | Lysosome vacuole | Golgi apparatus | Peroxisome |
---|---|---|---|---|---|---|---|---|---|---|---|
Cytoplasm|Nucleus | Nuclear localization signal|Peroxisomal targeting signal | 0.7755 | 0.7993 | 0.0359 | 0.0389 | 0.1412 | 0.0227 | 0.014 | 0.0616 | 0.0884 | 0.036 |
Orthofinder run ID | 4 |
Orthogroup | 2351 |
Change Orthofinder run |
Type of sequence | Sequence |
---|---|
Locus | Download genbank file of locus
Download genbank file of locus (reverse complement)
The gene with 5 kb flanks (if sufficient flanking sequence is available). For use in cloning design programs. NOTE: features (genes or exons) that are only partially contained within the sequence are completely excluded. |
Protein | >Hirsu2|3651 MGVRSVHGVPGDYNLVALDYLPECGLKWVGSVNELNAAYAADGYARVKSIAALVTTFGVGELSAINGMAGAFSEH IPVVHIVGCPSTISQRNGMLLHHTLGNGDFNVFANMNAQISCEVVKLNRPAEIADQIDHALRECWVSSRPVYVML PTDMVQSQIEGERLVTPIDLSEPRNEPEREDYVVDVAMKCLRAATRPVILVDSCAIRHRVLNEVHSLINKAGLPV FVTPMGKGAVDEQHPCYGGVYAGTGSFPIEVQNLVESSDLILTIGALKTDFNTTGFSYRTSQLNTIDLHSDHCVV RYSTYPGVRMRGVLRKMIDIIDVKDLSVQRSPVVKNEVQKNLDGSQTITQAWFWPRMGLFLDDNDVVVTETGTSN FGIWDTKFPSGVTALNQTLWGSIGWSVGACQGAALAVRDAGDNRRTILFVGDGSFQLTAQEVSTMIRLSLKPVIF VICNKGFTIERFIHGVDADYNDISVWQYKDIVDVFGGKQTCRKFVVKTKDELNVLLDDADFKSAACLQFVELHMP KMDAPRALVMTAEASAKNNARTD* |
Coding | >Hirsu2|3651 ATGGGCGTCCGTTCGGTCCATGGAGTTCCGGGCGATTACAACCTCGTCGCCCTCGACTATCTGCCAGAATGCGGC CTGAAGTGGGTTGGTAGCGTAAACGAACTCAACGCTGCCTATGCCGCCGATGGCTACGCTCGTGTTAAGAGTATC GCCGCCCTCGTTACCACCTTCGGAGTCGGTGAGCTTTCCGCCATCAACGGCATGGCCGGCGCCTTCTCGGAGCAT ATACCCGTCGTTCACATTGTCGGCTGCCCGTCCACGATCTCGCAGCGCAACGGCATGCTTCTTCATCATACGCTT GGCAACGGCGACTTCAACGTCTTCGCCAATATGAACGCCCAGATCTCGTGCGAGGTTGTCAAACTCAATCGGCCT GCCGAAATTGCCGATCAAATCGACCACGCGTTGCGCGAATGCTGGGTCTCCTCGCGCCCAGTGTACGTGATGCTA CCGACTGACATGGTCCAGAGCCAGATTGAGGGCGAGAGACTCGTGACTCCTATCGATCTCTCCGAGCCGCGGAAC GAACCCGAAAGAGAAGACTACGTTGTTGATGTAGCCATGAAGTGCCTCCGCGCTGCAACGCGCCCCGTCATTCTC GTTGACTCCTGTGCCATCCGCCACCGAGTCCTTAATGAGGTGCACAGTCTCATCAACAAGGCCGGCCTTCCTGTT TTCGTGACTCCCATGGGCAAGGGTGCTGTCGACGAGCAGCATCCCTGTTACGGCGGTGTCTACGCCGGGACTGGT TCTTTCCCCATCGAGGTCCAGAATCTCGTTGAGTCATCGGACCTTATTCTCACGATAGGCGCTCTCAAGACTGAC TTCAATACTACTGGCTTCTCCTATCGCACTTCGCAGCTCAACACTATCGATTTGCACAGCGATCATTGCGTGGTG AGATATTCGACCTATCCCGGCGTTCGCATGAGGGGTGTCTTGCGCAAGATGATCGACATCATCGATGTCAAGGAT CTCTCCGTCCAGAGGTCTCCAGTCGTAAAGAACGAAGTGCAGAAGAATCTCGACGGCTCGCAGACTATTACACAG GCCTGGTTCTGGCCTCGTATGGGGCTGTTCTTAGACGATAATGATGTGGTCGTGACAGAGACGGGGACTTCGAAC TTTGGCATCTGGGACACCAAGTTTCCGTCGGGCGTGACGGCGCTGAACCAAACCCTGTGGGGAAGTATAGGATGG TCCGTGGGCGCCTGTCAGGGTGCTGCCCTCGCCGTTCGAGACGCCGGTGATAACCGCAGAACTATCTTATTTGTC GGAGATGGGTCGTTTCAGCTGACAGCCCAGGAAGTGAGCACCATGATTCGCCTCAGCTTGAAGCCCGTAATTTTT GTCATTTGCAACAAGGGCTTTACCATCGAGCGCTTTATCCATGGTGTGGATGCAGATTATAACGACATATCAGTA TGGCAATACAAAGACATCGTGGACGTGTTTGGCGGCAAGCAAACGTGTCGCAAGTTCGTCGTCAAAACCAAGGAC GAACTGAATGTATTATTAGACGACGCCGACTTCAAGTCTGCAGCCTGTCTTCAGTTCGTTGAGCTGCATATGCCG AAGATGGACGCGCCACGGGCTTTGGTCATGACGGCGGAAGCGAGTGCCAAAAACAACGCGAGGACGGACTAG |
Transcript | >Hirsu2|3651 ATGGGCGTCCGTTCGGTCCATGGAGTTCCGGGCGATTACAACCTCGTCGCCCTCGACTATCTGCCAGAATGCGGC CTGAAGTGGGTTGGTAGCGTAAACGAACTCAACGCTGCCTATGCCGCCGATGGCTACGCTCGTGTTAAGAGTATC GCCGCCCTCGTTACCACCTTCGGAGTCGGTGAGCTTTCCGCCATCAACGGCATGGCCGGCGCCTTCTCGGAGCAT ATACCCGTCGTTCACATTGTCGGCTGCCCGTCCACGATCTCGCAGCGCAACGGCATGCTTCTTCATCATACGCTT GGCAACGGCGACTTCAACGTCTTCGCCAATATGAACGCCCAGATCTCGTGCGAGGTTGTCAAACTCAATCGGCCT GCCGAAATTGCCGATCAAATCGACCACGCGTTGCGCGAATGCTGGGTCTCCTCGCGCCCAGTGTACGTGATGCTA CCGACTGACATGGTCCAGAGCCAGATTGAGGGCGAGAGACTCGTGACTCCTATCGATCTCTCCGAGCCGCGGAAC GAACCCGAAAGAGAAGACTACGTTGTTGATGTAGCCATGAAGTGCCTCCGCGCTGCAACGCGCCCCGTCATTCTC GTTGACTCCTGTGCCATCCGCCACCGAGTCCTTAATGAGGTGCACAGTCTCATCAACAAGGCCGGCCTTCCTGTT TTCGTGACTCCCATGGGCAAGGGTGCTGTCGACGAGCAGCATCCCTGTTACGGCGGTGTCTACGCCGGGACTGGT TCTTTCCCCATCGAGGTCCAGAATCTCGTTGAGTCATCGGACCTTATTCTCACGATAGGCGCTCTCAAGACTGAC TTCAATACTACTGGCTTCTCCTATCGCACTTCGCAGCTCAACACTATCGATTTGCACAGCGATCATTGCGTGGTG AGATATTCGACCTATCCCGGCGTTCGCATGAGGGGTGTCTTGCGCAAGATGATCGACATCATCGATGTCAAGGAT CTCTCCGTCCAGAGGTCTCCAGTCGTAAAGAACGAAGTGCAGAAGAATCTCGACGGCTCGCAGACTATTACACAG GCCTGGTTCTGGCCTCGTATGGGGCTGTTCTTAGACGATAATGATGTGGTCGTGACAGAGACGGGGACTTCGAAC TTTGGCATCTGGGACACCAAGTTTCCGTCGGGCGTGACGGCGCTGAACCAAACCCTGTGGGGAAGTATAGGATGG TCCGTGGGCGCCTGTCAGGGTGCTGCCCTCGCCGTTCGAGACGCCGGTGATAACCGCAGAACTATCTTATTTGTC GGAGATGGGTCGTTTCAGCTGACAGCCCAGGAAGTGAGCACCATGATTCGCCTCAGCTTGAAGCCCGTAATTTTT GTCATTTGCAACAAGGGCTTTACCATCGAGCGCTTTATCCATGGTGTGGATGCAGATTATAACGACATATCAGTA TGGCAATACAAAGACATCGTGGACGTGTTTGGCGGCAAGCAAACGTGTCGCAAGTTCGTCGTCAAAACCAAGGAC GAACTGAATGTATTATTAGACGACGCCGACTTCAAGTCTGCAGCCTGTCTTCAGTTCGTTGAGCTGCATATGCCG AAGATGGACGCGCCACGGGCTTTGGTCATGACGGCGGAAGCGAGTGCCAAAAACAACGCGAGGACGGACTAG |
Gene | >Hirsu2|3651 ATGGGCGTCCGTTCGGTCCATGGAGTTCCGGGCGATTACAACCTCGTCGCCCTCGACTATCTGCCAGAATGCGGC CTGAAGTGGGTTGGTAGCGTAAACGAACTCAACGCTGGTGAGTCTGCGGCCCTCGCGTTCCGCTGTTCCGGGCTC GTCCCTAGCTGACGGCACATCATGCACGAGCCTATGCCGCCGATGGCTACGCTCGTGTTAAGAGTATCGCCGCCC TCGTTACCACCTTCGGAGTCGGTGAGCTTTCCGCCATCAACGGCATGGCCGGCGCCTTCTCGGAGCATATACCCG TCGTTCACATTGTCGGCTGCCCGTCCACGATCTCGCAGCGCAACGGCATGCTTCTTCATCATACGCTTGGCAACG GCGACTTCAACGTCTTCGCCAATATGAACGCCCAGATCTCGTGCGAGGTTGTCAAACTCAATCGGCCTGCCGAAA TTGCCGATCAAATCGACCACGCGTTGCGCGAATGCTGGGTCTCCTCGCGCCCAGTGTACGTGATGCTACCGACTG ACATGGTCCAGAGCCAGATTGAGGGCGAGAGACTCGTGACTCCTATCGATCTCTCCGAGCCGCGGAACGAACCCG AAAGAGAAGACTACGTTGTTGATGTAGCCATGAAGTGCCTCCGCGCTGCAACGCGCCCCGTCATTCTCGTTGACT CCTGTGCCATCCGCCACCGAGTCCTTAATGAGGTGCACAGTCTCATCAACAAGGCCGGCCTTCCTGTTTTCGTGA CTCCCATGGGCAAGGGTGCTGTCGACGAGCAGCATCCCTGTTACGGCGGTGTCTACGCCGGGACTGGTTCTTTCC CCATCGAGGTCCAGAATCTCGTTGAGTCATCGGACCTTATTCTCACGATAGGCGCTCTCAAGGTGCTCTGATTGA CCCATCTGCGTTACTGAATGCGGAACTTGTCGCGGCTAACTTGGATCAATCTGCAGACTGACTTCAATACTACTG GCTTCTCCTATCGCACTTCGCAGCTCAACACTATCGATTTGCACAGCGATCATTGCGTGGTGAGATATTCGACCT ATCCCGGCGTTCGCATGAGGGGTGTCTTGCGCAAGATGATCGACATCATCGATGTCAAGGATCTCTCCGTCCAGA GGTCTCCAGTCGTAAAGAACGAAGTGCAGAAGAATCTCGACGGCTCGCAGACTATTACACAGGCCTGGTTCTGGC CTCGTATGGGGCTGTTCTTAGACGATAATGATGTGGTCGTGACAGAGACGGGGACTTCGAACTTTGGCATCTGGG ACACCAAGTTTCCGTCGGGCGTGACGGCGCTGAACCAAACCCTGTGGGGAAGTATAGGATGGTCCGTGGGCGCCT GTCAGGGTGCTGCCCTCGCCGTTCGAGACGCCGGTGATAACCGCAGAACTATCTTATTTGTCGGAGATGGGTCGT TTCAGCTGACAGCCCAGGAAGTGAGCACCATGATTCGCCTCAGCTTGAAGCCCGTAATGTGAGTCCCCTTAAGAC AGTGATATCTCCACACCGCTCCGTCCGCCCCTTTCCCGAGGGAAGAAACAAAAGGGTGAGAAGAAAAGATAGCGA CGGCGCAGACATAACTCATATAGAGGAAAAGCTCTGTGCCATGGCTGACTGTCTGAGGAAAGTTTTGTCATTTGC AACAAGGGCTTTACCATCGAGCGCTTTATCCATGGTGTGGATGCAGATTATAACGACATATCAGTATGGCAATAC AAAGACATCGTGGACGTGTTTGGCGGCAAGCAAACGTGTCGCAAGTTCGTCGTCAAAACCAAGGACGAACTGAAT GTATTATTAGACGACGCCGACTTCAAGTCTGCAGCCTGTCTTCAGTTCGTTGAGCTGCATATGCCGAAGATGGAC GCGCCACGGGCTTTGGTCATGACGGCGGAAGCGAGTGCCAAAAACAACGCGAGGACGGACTAG |